Castagna C, Ball G F, Balthazart J
European Graduate School for Neuroscience, University of Liège, Laboratory of Biochemistry, Belgium.
Pharmacol Biochem Behav. 1997 Oct;58(2):403-14. doi: 10.1016/s0091-3057(97)00243-8.
The effects of pharmacological manipulations of dopaminergic transmission on appetitive and consummatory aspects of male sexual behavior were investigated in castrated male Japanese quail treated with exogenous testosterone. Appetitive male sexual behavior was assessed by measuring a learned social proximity response and consummatory behavior was assessed by measuring copulatory behavior per se. The nonselective dopamine receptor agonist, apomorphine, inhibited in a dose-dependent manner both components of male sexual behavior. Two indirect dopamine agonists were also tested. Nomifensine, a dopamine re-uptake inhibitor, decreased appetitive sexual behavior but increased the frequency of mount attempts, a measure of consummatory sexual behavior. Amfonelic acid, a compound that enhances dopaminergic tone by a complex mechanism, increased aspects of both appetitive and consummatory behaviors. These data suggest that, in quail, as in rodents, increases in dopaminergic tone facilitate both appetitive and consummatory aspects of male sexual behavior. Apomorphine may be inhibitory in quail because it acts primarily on D2-like receptors, unlike in rats, where it stimulates sexual behavior and acts primarily on D1-like receptors at low doses but interacts with D2-like receptors at higher doses. This is supported by the observation that stereotyped pecking, a behavior stimulated selectively in quail by D2 agonists, was increased by apomorphine but not by the two indirect agonists. The observed partial dissociation between the effects of these dopaminergic agonists on appetitive and consummatory sexual behaviors suggests that these two components of male sexual behavior may be controlled by the action of dopamine through different neuronal systems.
在接受外源性睾酮治疗的去势雄性日本鹌鹑中,研究了多巴胺能传递的药理学操作对雄性性行为的欲求方面和完成方面的影响。通过测量习得的社会接近反应来评估雄性性行为的欲求方面,通过测量交配行为本身来评估完成方面。非选择性多巴胺受体激动剂阿扑吗啡以剂量依赖性方式抑制雄性性行为的两个组成部分。还测试了两种间接多巴胺激动剂。诺米芬辛是一种多巴胺再摄取抑制剂,它减少了欲求性性行为,但增加了爬跨尝试的频率,这是一种完成性性行为的指标。氨苯磺酸是一种通过复杂机制增强多巴胺能张力的化合物,它增加了欲求性和完成性性行为的多个方面。这些数据表明,在鹌鹑中,与啮齿动物一样,多巴胺能张力的增加促进了雄性性行为的欲求方面和完成方面。阿扑吗啡在鹌鹑中可能具有抑制作用,因为它主要作用于D2样受体,这与大鼠不同,在大鼠中,它在低剂量时刺激性行为,主要作用于D1样受体,但在高剂量时与D2样受体相互作用。这一观点得到了以下观察结果的支持:刻板啄食是一种由D2激动剂在鹌鹑中选择性刺激的行为,阿扑吗啡增加了这种行为,但两种间接激动剂没有。这些多巴胺能激动剂对欲求性和完成性性行为的影响之间观察到的部分分离表明,雄性性行为的这两个组成部分可能由多巴胺通过不同的神经元系统控制。